Nesma M Elaraby

4PUBLICATIONS
0CO-AUTHORS
Gene mappingMedical molecular engineering of nucleic acids and proteinsSociolinguisticsArtificial life and complex adaptive systems
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Publications (4)

|Jun 14, 2024
Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients.

Nesma M Elaraby, Hoda A Ahmed, Heba Dawoud

|May 31, 2024
Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene.

Nesma M Elaraby, Hoda A Ahmed, Neveen A Ashaat

|Jul 20, 2023
First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease.

Nesma M Elaraby, Eman Reda Galal, Mohamed Abdel-Hamid

|Oct 17, 2022
Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature.

Nesma M Elaraby, Hoda A Ahmed, Neveen A Ashaat

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